Label: MEDIORO W- olive oi l spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated November 3, 2021

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  • ACTIVE INGREDIENT

    Olive oil 1.20%

  • PURPOSE

    Antibacterial, Odor care

  • Uses

    ■ Antibacterial and anti-inflammatory effects help prevent vaginitis.
    ■ Relieves external itching and alleviates odors before and after the menstruation

  • WARNINGS

    For vaginal use only
    If the area of use has abnormal symptoms or side effects such as red spots, swelling, or iching, consult a specialist.
    Do not use it in areas with wounds.
    Don’t use it right after removing the fur.
    Keep out of reach of children

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Directions

    ■ Spray lightly about 5cm away from the area of use.
    ■ You can use if from time to time if necessary.

  • Other Information

    ■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

  • Questions

    ■ www.medioro.shop / +82) 0507-1390-9493 / medifun35600@gmail.com

  • INACTIVE INGREDIENTS

    Water, Chamaecyparis Obtusa Water, 1,2-Hexanediol, PEG-60 Hydrogenated Castor Oil, PEG-100 Stearate, Glyceryl Stearate, Disodium EDTA, Lavandula Angustifolia (Lavender) Oil, Sorbitan Sesquioleate, Citrus Nobilis (Mandarin Orange) Oil, Damascena Flower Oil

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    MEDIORO W 
    olive oi l spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82363-010
    Route of AdministrationVAGINAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OLIVE OIL (UNII: 6UYK2W1W1E) (OLIVE OIL - UNII:6UYK2W1W1E) OLIVE OIL0.12 g  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    CHAMAECYPARIS OBTUSA WOOD OIL (UNII: P2OMP71Y62)  
    1,2-Hexanediol (UNII: TR046Y3K1G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82363-010-021 in 1 CARTON10/01/2021
    1NDC:82363-010-0110 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/2021
    Labeler - MEDIFUN Inc. (695722552)
    Registrant - MEDIFUN Inc. (695722552)
    Establishment
    NameAddressID/FEIBusiness Operations
    MEDIFUN Inc.695722552manufacture(82363-010)
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